Rapidpoint 405, 500 And Rapidlab 1245 Blood Gas Analyzer (2018-07-24)

Recall Summary Siemens Healthineers is recalling RAPIDPoint 405, 500 and RAPIDLab 1245 blood gas analyzers distributed across Canada because these devices may produce inaccurate test results due to a software issue. The analyzers are used in hospitals and clinical laboratories to measure blood oxygen, carbon dioxide, and pH levels. This is a Class I recall, meaning there is a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-08-17

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2b9b6903-d4e5-472e-84ad-9c489496339b